Data Foundry

Drug recalls 2023

Dianeal Low Calcium — Class II drug recall D-0542-2023

Completed recall by Baxter Healthcare Corporation, reported 2023-05-03, distributed nationwide. Lack of Assurance of Sterility: Potential presence of leaks originating from the Luer component.

Recall numberD-0542-2023
Product typeDrug
ClassificationClass II
StatusCompleted
Voluntary or mandatedVoluntary
Recalling firmBaxter Healthcare Corporation, Deerfield, IL, United States
Recall initiated2023-03-15
Classified2023-04-24
Reported by FDA2023-05-03
DistributedNationwide (US)
Reason classessterility, packaging
NDC00941-0409, 00941-0409-01, 00941-0409-05, 00941-0409-06, 00941-0409-07, 00941-0411, 00941-0411-04, 00941-0411-05, 00941-0411-06, 00941-0411-07, 00941-0411-11, 00941-0413, 00941-0413-01, 00941-0413-04, 00941-0413-05, 00941-0413-06, 00941-0413-07, 00941-0415, 00941-0415-01, 00941-0415-04, 00941-0415-05, 00941-0415-06, 00941-0415-07, 00941-0424, 00941-0424-51 and 35 more
Lot numbersY406314, Y406314A, Y406963, Y407199
Expiration dates2024-10-31

Product

Dianeal Low Calcium (2.5 mEq/L) Peritonial Dialysis Solution with 1.5% Dextrose, packaged in a) 5000 mL per Ambu-Flex II Container bag, Product Code L5B4826, NDC 0941-0409-07; and b) 6000 mL per Ambu-Flex II Container bag, Product Code L5B9770, NDC 0941-0409-01, Rx Only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA.

Reason for recall

Lack of Assurance of Sterility: Potential presence of leaks originating from the Luer component.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0542-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.